FDA Inspection 1125537 — Siegfried St. Vulbas SAS

Siegfried St. Vulbas SAS — FEI 3002807787

The FDA completed an inspection of Siegfried St. Vulbas SAS on Nov 7, 2019 in Saint-Vulbas. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 7, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint-Vulbas (France)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.